Run ID: ERR4818340
Sample name:
Date: 01-04-2023 15:30:16
Number of reads: 200679
Percentage reads mapped: 97.08
Strain: lineage5.3
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage5.3 | West-Africa 1 | AFRI_2;AFRI_3 | RD711 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 6446 | p.Ala403Ser | missense_variant | 1.0 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 9143 | c.1842T>C | synonymous_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
gyrA | 9566 | c.2265C>T | synonymous_variant | 1.0 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
mshA | 575284 | c.-64C>A | upstream_gene_variant | 0.5 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 775764 | p.Val906Ala | missense_variant | 0.25 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
mmpL5 | 776339 | p.His714Gln | missense_variant | 0.25 |
mmpL5 | 776371 | p.Gly704Cys | missense_variant | 0.29 |
mmpL5 | 778213 | p.Ala90Pro | missense_variant | 0.33 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781763 | c.204C>A | synonymous_variant | 0.4 |
rplC | 800793 | c.-16G>C | upstream_gene_variant | 1.0 |
fbiC | 1302899 | c.-32A>G | upstream_gene_variant | 1.0 |
Rv1258c | 1406946 | p.Ala132Asp | missense_variant | 0.25 |
inhA | 1673338 | c.-864G>A | upstream_gene_variant | 1.0 |
fabG1 | 1673343 | c.-96delC | upstream_gene_variant | 0.33 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2101921 | c.1122G>A | synonymous_variant | 1.0 |
ndh | 2102299 | p.Met248Ile | missense_variant | 0.4 |
ndh | 2102846 | p.Gly66Glu | missense_variant | 0.25 |
ndh | 2103112 | c.-70G>T | upstream_gene_variant | 1.0 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
PPE35 | 2167675 | p.Leu980Met | missense_variant | 0.67 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2168255 | c.2358G>A | synonymous_variant | 0.4 |
PPE35 | 2170073 | c.540C>A | synonymous_variant | 0.22 |
PPE35 | 2170643 | c.-31G>A | upstream_gene_variant | 0.33 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289338 | c.-97A>G | upstream_gene_variant | 0.29 |
pncA | 2290020 | c.-780delC | upstream_gene_variant | 0.29 |
pncA | 2290062 | c.-821G>A | upstream_gene_variant | 1.0 |
kasA | 2518132 | c.18C>T | synonymous_variant | 1.0 |
eis | 2715036 | c.297G>T | synonymous_variant | 0.25 |
ahpC | 2726531 | p.Asp113Glu | missense_variant | 0.4 |
pepQ | 2859519 | c.900G>A | synonymous_variant | 0.4 |
ribD | 2987177 | c.339A>G | synonymous_variant | 0.33 |
Rv2752c | 3064931 | c.1261C>T | synonymous_variant | 0.67 |
thyA | 3074621 | c.-150T>A | upstream_gene_variant | 0.5 |
ald | 3087081 | p.Gly88Arg | missense_variant | 1.0 |
ald | 3087084 | c.266delA | frameshift_variant | 1.0 |
ald | 3087184 | c.368_373delCCGACG | disruptive_inframe_deletion | 1.0 |
ald | 3087879 | p.Arg354Trp | missense_variant | 0.33 |
Rv3083 | 3449012 | p.Pro170Leu | missense_variant | 1.0 |
Rv3083 | 3449910 | c.1407C>T | synonymous_variant | 0.67 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
whiB7 | 3568462 | p.Gln73Leu | missense_variant | 0.25 |
whiB7 | 3568519 | p.Ala54Asp | missense_variant | 0.22 |
fbiA | 3640394 | c.-149G>A | upstream_gene_variant | 1.0 |
fbiB | 3642285 | p.Leu251Val | missense_variant | 0.18 |
alr | 3840367 | p.Pro352Ser | missense_variant | 1.0 |
rpoA | 3877590 | c.918G>T | synonymous_variant | 0.4 |
rpoA | 3877737 | c.771G>C | synonymous_variant | 0.25 |
rpoA | 3877743 | c.765T>C | synonymous_variant | 0.25 |
rpoA | 3877748 | c.760C>T | synonymous_variant | 0.25 |
rpoA | 3877764 | c.744C>G | synonymous_variant | 0.4 |
rpoA | 3877770 | c.738A>G | synonymous_variant | 0.4 |
rpoA | 3877776 | c.732T>C | synonymous_variant | 0.4 |
rpoA | 3877782 | c.726T>C | synonymous_variant | 0.5 |
rpoA | 3877797 | c.711G>A | synonymous_variant | 0.5 |
rpoA | 3877803 | c.705G>C | synonymous_variant | 0.5 |
ddn | 3986987 | c.144G>T | synonymous_variant | 1.0 |
ddn | 3987180 | p.Asp113Asn | missense_variant | 1.0 |
clpC1 | 4039116 | p.Lys530Met | missense_variant | 1.0 |
clpC1 | 4040824 | c.-120C>T | upstream_gene_variant | 1.0 |
panD | 4044171 | p.Asp37Glu | missense_variant | 1.0 |
panD | 4044297 | c.-16C>A | upstream_gene_variant | 0.4 |
embC | 4239843 | c.-20A>C | upstream_gene_variant | 1.0 |
embC | 4240671 | p.Thr270Ile | missense_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4244220 | c.988C>T | synonymous_variant | 1.0 |
embA | 4244635 | p.Val468Ala | missense_variant | 1.0 |
embA | 4244768 | p.Glu512Asp | missense_variant | 0.29 |
embA | 4245090 | p.Gly620Ser | missense_variant | 0.5 |
embA | 4245147 | p.Pro639Ser | missense_variant | 1.0 |
embB | 4247646 | p.Glu378Ala | missense_variant | 1.0 |
aftB | 4267168 | p.Gln557Glu | missense_variant | 0.4 |
aftB | 4267425 | p.Gly471Glu | missense_variant | 0.22 |
aftB | 4268171 | c.666G>C | synonymous_variant | 0.67 |
aftB | 4268179 | c.658T>C | synonymous_variant | 0.67 |
aftB | 4268183 | c.654A>T | synonymous_variant | 0.67 |
aftB | 4268194 | p.Leu215Val | missense_variant | 0.4 |
aftB | 4268207 | c.630C>G | synonymous_variant | 0.4 |
aftB | 4268213 | c.624T>C | synonymous_variant | 0.33 |
aftB | 4268219 | c.618C>G | synonymous_variant | 0.29 |
aftB | 4268228 | c.609C>G | synonymous_variant | 0.29 |
aftB | 4268258 | c.579C>T | synonymous_variant | 0.22 |
ubiA | 4269387 | p.Glu149Asp | missense_variant | 1.0 |
aftB | 4269606 | c.-770T>C | upstream_gene_variant | 1.0 |
ethA | 4327103 | p.Gly124Asp | missense_variant | 1.0 |
ethA | 4327532 | c.-59G>T | upstream_gene_variant | 0.4 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
whiB6 | 4338620 | c.-99G>A | upstream_gene_variant | 0.33 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |